Assist to lead 45 members of QA Team and QA Compliance

 Establishment of BPR, BMR, SOPs & all other necessary documents,  Preparation and Update of Training Manual and Conduct Training Program as Trainer, Supervise process validation/ Cleaning validation/ Qualification (IQ/OQ/PQ)/ Revalidation, Coordinate the validation of cleaning procedures of manufacturing equipments. Establish all In process documents and Supervise the daily In-process Check,  Supervise & coordinate all QA or compliance & validation documents/ Records/… Show more  Establishment of BPR, BMR, SOPs & all other necessary documents,  Preparation and Update of Training Manual and Conduct Training Program as Trainer, Supervise process validation/ Cleaning validation/ Qualification (IQ/OQ/PQ)/ Revalidation, Coordinate the validation of cleaning procedures of manufacturing equipments. Establish all In process documents and Supervise the daily In-process Check,  Supervise & coordinate all QA or compliance & validation documents/ Records/ BMR & BPR in line with proper documentation & retrieval system. Supervise, monitoring and approval the QC analytical test report by HPLC, FTIR, UV, Dissolution etc for Raw Material, Packing Material and Finished Product also,  Environment & ETP Monitoring, Implement & maintain hygiene safety regulations. Ensure quality raw materials are received as well as contribute to the quality delivery of factory production, achieving quality targets and standards. Managing & executing production operations Document /BPR/ BMR/ compilation, checking, archiving, retrieving (when necessary) and disposal of expired documents. Preparation of Certificate of Analysis for finished formulated products. Handling of retention sample, storage and disposal of expiry date retention sample.  Monitoring of new source materials. Maintain Customer Complained Handling,  Visit and monitoring the Quality Issues of Distribution Store, Show less

 GMP and SOP implementation activities.  Sampling of Raw, Packaging materials and products (intermediates and finished stage). Handling of new source raw material,  QA inspection during dispensing of Raw materials. In-process inspection and line clearance in production area of liquid, solid, packaging, antibiotic, MDI department. Preparation of Certificate of Analysis for finished formulated products. Environment Monitoring,  Document /BPR/ BMR/ compilation,… Show more  GMP and SOP implementation activities.  Sampling of Raw, Packaging materials and products (intermediates and finished stage). Handling of new source raw material,  QA inspection during dispensing of Raw materials. In-process inspection and line clearance in production area of liquid, solid, packaging, antibiotic, MDI department. Preparation of Certificate of Analysis for finished formulated products. Environment Monitoring,  Document /BPR/ BMR/ compilation, checking, archiving, retrieving (when necessary) and disposal of expired documents. Perform validation activity according to validation protocol,  Perform calibration activity as calibration schedule.  Handling of retention sample, storage and disposal of expiry date retention sample.  Monitoring of new source materials. Any other quality related activities as and when advised. Maintain & updating of SOPs & many other document, Customer complain handling,  Preparation, updating & maintain validation protocol, Perform & maintain routine calibration of critical control equipment & also check daily environ control monitoring parameter,  Attained & also perform on job training program etc Show less

The responsibilities of BEXIMCO Phama as Officer, Quality Assurance was same as the responsibilities of Popular Pharma as Officer, QA.